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PMID: 12493010 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

Fc receptor homologs: newest members of a remarkably diverse Fc receptor gene family.

Immunological reviews ·Vol. 190 ·2002-12-00 ·Pages 123-36

Davis RS, Dennis G, Odom MR, Gibson AW, Kimberly RP, Burrows PD, Cooper MD

Abstract

Newfound relatives of the classical Fc receptors (FcR) have been provisionally named the Fc receptor homologs (FcRH). The recent identification of eight human and six mouse FcRH genes substantially increases the size and functional potential of the FcR family. The extended family of FcR and FcRH genes spans approximately 15 Mb of the human chromosome 1q21-23 region, whereas in mice this family is split between chromosomes 1 and 3. The FcRH genes encode molecules with variable combinations of five subtypes of immunoglobulin (Ig) domains. The presence of a conserved sequence motif in one Ig domain subtype implies Ig Fc binding capability for many FcRH family members that are preferentially expressed by B lineage cells. In addition, most FcRH family members have consensus tyrosine-based activating and inhibitory motifs in their cytoplasmic domains, while the others lack features typical of transmembrane receptors. The FcRH family members, like the classical FcRs, come in multiple isoforms and allelic variations. The unique individual and polymorphic properties of the FcR/FcRH members indicate a remarkably diverse Fc receptor gene family with immunoregulatory function.

MeSH Terms
Amino Acid Sequence Animals Chromosomes, Human, Pair 1/genetics Genetic Variation Humans Mice Molecular Sequence Data Multigene Family Phylogeny Polymorphism, Genetic Protein Sorting Signals/genetics Protein Structure, Tertiary Receptors, Fc/chemistry,genetics Sequence Homology, Amino Acid Species Specificity
Chemicals
Protein Sorting Signals Receptors, Fc
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Davis Randall S
Division of Hematology/Oncology, University of Alabama at Birmingham, AL 35294, USA.
Dennis Glynn
Odom Mary R
Gibson Andrew W
Kimberly Robert P
Burrows Peter D
Cooper Max D
Article Info
Journal
Immunological reviews
Abbr.
Immunol Rev
ISSN
0105-2896
Published
2002-12-00
Pages
123-36
Language
English
Region
England
NLM ID
7702118
Subset
IM
Grants
NIAID NIH HHS · AI39816 · United States
NIAID NIH HHS · AI48098 · United States
NIAMS NIH HHS · AR49084 · United States
NIDDK NIH HHS · DK07488 · United States
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